Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10435719 8 11919395 downstream gene variant C/T snv 0.48 2
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 2
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 2
rs10744775
BRAP
12 111658411 intron variant T/C snv 0.44 2
rs10778215
C12orf42
12 103143488 intron variant T/A;G snv 2
rs10838687
MADD
11 47291341 intron variant T/G snv 0.31 2
rs11208722 1 65705318 intron variant C/A snv 0.75 2
rs1127311
ADAR ; CHRNB2
1 154584187 3 prime UTR variant G/A snv 0.42 2
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 2
rs116971887
LOC105371253 ; SALL1
16 51136115 3 prime UTR variant G/T snv 3.1E-02 2
rs11874381
LOC105372112
18 49677038 intergenic variant G/A snv 0.32 2
rs12711751 2 113080188 downstream gene variant T/G snv 0.61 2
rs12741825 1 159700355 downstream gene variant C/T snv 0.24 2
rs12742376
KDF1
1 26958704 intron variant C/T snv 6.8E-02 2
rs12755606 1 159700546 downstream gene variant C/G snv 0.24 2
rs13409360 2 113080525 downstream gene variant G/A snv 0.38 2
rs1441759 8 20008052 intergenic variant G/C snv 2.9E-02 2
rs17597773
HLX-AS1 ; HLX
1 220881419 non coding transcript exon variant C/G snv 0.25 0.23 2
rs17688076
PLA2G15
16 68252524 intron variant C/A snv 0.14 0.11 2
rs1880241
STEAP1B
7 22719850 intron variant A/G snv 0.51 2
rs1998303 9 82800066 intergenic variant A/G snv 0.37 2
rs2277844
PLA2G6
22 38181508 intron variant G/A snv 0.53 2
rs2285810
HECTD4
12 112261736 non coding transcript exon variant T/C snv 0.45 2
rs2307246
PLA2G2A
1 19978364 non coding transcript exon variant G/A snv 0.18 0.18 2
rs2686555
CABP1
12 120657369 intron variant A/G snv 0.52 2